Oxybutynin Chloride
- Product NDC
- 50090-6967
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Oxybutynin Chloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA209823
- Marketing category
- ANDA
- Substance
- OXYBUTYNIN CHLORIDE
- Current FDA listing
- Yes
Related Records
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|---|---|---|---|---|
| 50090-6967-0 | 90 TABLET in 1 BOTTLE (50090-6967-0) | 2023-12-21 | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|---|---|---|---|
| Oxybutynin Chloride Tablets, USP Rx only | A-S Medication Solutions | 2023-12-27 | Human Prescription Drug Label | 1 |